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496807-11-5

中文名稱 sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate
英文名稱 sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate
CAS 496807-11-5
分子式 C24H31NaO5
分子量 422.5
MOL 文件 496807-11-5.mol
更新日期 2025/10/09 16:48:51
496807-11-5 結(jié)構(gòu)式 496807-11-5 結(jié)構(gòu)式

基本信息

中文別名
(RAC)-貝拉前列素鈉
貝拉前列素鈉鹽(非對(duì)映異構(gòu)體混合物)
英文別名
Beraprost sodium (Relative stereochemistry)
sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO: 250 mg/mL (594.57 mM)
形態(tài)Solid
顏色White to light yellow

常見(jiàn)問(wèn)題列表

生物活性
Beraprost sodium 是一種前列環(huán)素類似物,是一種穩(wěn)定且具有口服活性的 PGI2 前藥。Beraprost sodium 是有效的血管擴(kuò)張劑 (vasodilator),通過(guò)擴(kuò)張腎血管,改善微循環(huán)而具有研究肺動(dòng)脈高壓的潛力。
靶點(diǎn)

prodrug of PGI2; Vasodilator

體外研究

Beraprost sodium (0.1, 1.0, and 10.0?μM; 24 hours) treatment leads to a significant increase in the number of tube formation, BPS plays an important role on angiogenic activity. Beraprost sodium (0.1, 1.0, and 10.0?μM; 24 hours) treatment let VE-cadherin at regions of cell–cell contact becomes more abundant and the morphology of endothelial cells tends to be normal compared with those cultured under hypoxia conditions.

體內(nèi)研究

Beraprost sodium (oral adminstration; 0.6?mg/kg; once daily; 3 or 7 days) can mitigate the development of renal interstitial fibrosis, decrease renal oxidative stress through its potential vasodilation effect, and further prevent renal interstitial fibrosis.

Animal Model: 6-8-week-old C57Bl/6J Male Mice
Dosage: 0.6?mg/kg
Administration: Oral adminstration; 0.6?mg/kg; once daily; 3 or 7 days
Result: Mitigated the development of renal interstitial fibrosis.
"496807-11-5" 相關(guān)產(chǎn)品信息
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